Canonical Allele Identifier: CA136862356
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs373826500

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269807_31269808del , CM000668.2:g.31269807_31269808del GRCh38
NC_000006.11:g.31237584_31237585del , CM000668.1:g.31237584_31237585del GRCh37
NC_000006.10:g.31345563_31345564del NCBI36
NG_029422.2:g.7324_7325del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+158_1015+159del MANE Select ENSP00000365402.5:n.1015+158_1015+159del
ENST00000376228.9:c.1015+158_1015+159del ENSP00000365402.5:n.1015+158_1015+159del
ENST00000376237.8:c.*602+158_*602+159del ENSP00000365412.4:n.*602+158_*602+159del
ENST00000383329.7:c.1015+158_1015+159del ENSP00000372819.3:n.1015+158_1015+159del
ENST00000470363.5:n.491_492del
ENST00000487245.5:n.1374+158_1374+159del
NM_002117.5:c.1015+158_1015+159del NP_002108.4:n.1015+158_1015+159del
NM_002117.6:c.1015+158_1015+159del MANE Select NP_002108.4:n.1015+158_1015+159del